Fenofibrate and the kidney: an overview

作者: Michael S Kostapanos , Matilda Florentin , Moses S Elisaf , None

DOI: 10.1111/ECI.12068

关键词: EndocrinologyCreatinineKidneyFenofibrateGlomerulosclerosisAlbuminuriaRenal functionMedicineNephrotoxicityRenal blood flowInternal medicineClinical biochemistryBiochemistryGeneral Medicine

摘要: Background Fenofibrate has been used for the management of atherogenic dyslipidaemia many years. Reports fenofibrate-associated increases in serum creatinine (SCr) levels raised concerns regarding deleterious effects on renal function. Design In this narrative review, we discuss available literature effect fenofibrate kidney. Results Most clinical studies showed a rapid (within weeks) raising SCr levels. This was often accompanied by declined estimated glomerular filtration rate. Risk predictors adverse might include increased age, impaired function and high-dose treatment. Also, concomitant use medications affecting hemodynamics (e.g. angiotensin-converting enzyme-inhibitors (ACEi) angiotensin receptor blockers) may predispose to Interestingly, were transient reversible even without treatment discontinuation. Furthermore, associated with slower progression impairment albuminuria long-term basis. be protective against pathological changes diabetic nephropathy hypertensive glomerulosclerosis. In context, it is uncertain whether increase mirrors true deterioration. Several theories have expressed. The most dominant one involved inhibition vasodilatory prostaglandins reducing plasma flow pressure. Increased secretion or reduced clearance also suggested. These hypotheses should settled further studies. Conclusions Fenofibrate not nephrotoxic drug. However, close monitoring relevant especially high-risk patients. Increases ≥30% can impose

参考文章(89)
N el Esper, A Pruna, C Hottelart, J M Achard, A Fournier, [Fenofibrate increases blood creatinine, but does not change the glomerular filtration rate in patients with mild renal insufficiency]. Nephrologie. ,vol. 20, pp. 41- 44 ,(1999)
Bargman Jm, Lipscombe J, Lewis Gf, Cattran D, Deterioration in renal function associated with fibrate therapy. Clinical Nephrology. ,vol. 55, pp. 39- 44 ,(2001)
O Djurdjev, L Duncan, A Levin, R J Shapiro, R Dumas, S Ross, J Frohlich, A Belanger, A randomized placebo-controlled double-blind trial of lipid lowering strategies in patients with renal insufficiency: diet modification with or without fenofibrate Clinical Nephrology. ,vol. 53, pp. 140- 146 ,(2000)
Effects of intensive glucose lowering in type 2 diabetes The New England Journal of Medicine. ,vol. 358, pp. 2545- 2559 ,(2008) , 10.1056/NEJMOA0802743
Alain Meyrier, Hypertensive nephrosclerosis pathogenesis, diagnosis and management. Saudi Journal of Kidney Diseases and Transplantation. ,vol. 10, pp. 267- 274 ,(1999)
Richard J. Roman, P-450 Metabolites of Arachidonic Acid in the Control of Cardiovascular Function Physiological Reviews. ,vol. 82, pp. 131- 185 ,(2002) , 10.1152/PHYSREV.00021.2001
Theodosios D Filippatos, None, A review of time courses and predictors of lipid changes with fenofibric acid-statin combination. Cardiovascular Drugs and Therapy. ,vol. 26, pp. 245- 255 ,(2012) , 10.1007/S10557-012-6394-0
Jean-Claude Ansquer, Christelle Foucher, Stephanie Rattier, Marja-Riitta Taskinen, George Steiner, Fenofibrate reduces progression to microalbuminuria over 3 years in a placebo-controlled study in type 2 diabetes: results from the Diabetes Atherosclerosis Intervention Study (DAIS). American Journal of Kidney Diseases. ,vol. 45, pp. 485- 493 ,(2005) , 10.1053/J.AJKD.2004.11.004